EP3063104A1 - Ceramic article and method therefor using particle infiltration and preceramic polymer infiltration - Google Patents
Ceramic article and method therefor using particle infiltration and preceramic polymer infiltrationInfo
- Publication number
- EP3063104A1 EP3063104A1 EP14858836.1A EP14858836A EP3063104A1 EP 3063104 A1 EP3063104 A1 EP 3063104A1 EP 14858836 A EP14858836 A EP 14858836A EP 3063104 A1 EP3063104 A1 EP 3063104A1
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- Prior art keywords
- particles
- porosity
- intra
- bundle porosity
- bundle
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/565—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide
- C04B35/571—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide obtained from Si-containing polymer precursors or organosilicon monomers
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Definitions
- Ceramic articles can be produced using any of various known ceramic processing techniques.
- One example structure includes a ceramic matrix and fibers that are dispersed in the matrix (ceramic matrix composite or "CMC").
- the matrix can be deposited among the fibers using a polymer-infiltration-pyrolysis (“PIP") process, for example.
- PIP polymer-infiltration-pyrolysis
- the PIP process typically involves infiltrating a fiber structure with a preceramic polymer, and then thermally converting the preceramic polymer to ceramic material. The infiltration process can be repeated to achieve a desired density in the structure.
- this and other known ceramic processing techniques can result in deficiencies, such as incomplete densification, microcracking and residual unreacted material. These deficiencies can later debit the properties of the structure, such as long term oxidative stability , environmental durability and mechanical properties
- a method of fabricating a ceramic article includes providing a porous body that includes a plurality of fiber bundles that has an intra-bundle porosity and an inter-bundle porosity, infiltrating the intra-bundle porosity and the inter-bundle porosity with a mixture of particles in a liquid carrier, the particles having an average size selected with respect to at least the intra-bundle porosity, removing the liquid carrier from the porous body to deposit the particles in the intra-bundle porosity and in the inter-bundle porosity, infiltrating a preceramic polymer into a remaining intra-bundle porosity and a remaining inter-bundle porosity, and thermally converting the preceramic polymer to a ceramic material.
- the particles include ceramic -based particles.
- the ceramic -based particles and the ceramic material have equivalent composition.
- the equivalent composition is silicon carbide (SiC).
- the average size of the particles is selected with respect to a size factor of the intra-bundle porosity such that the particles can fit into the intra-bundle porosity.
- the average size of the particles is selected with respect to a threshold size above which the particles substantially block infiltration into the intra-bundle porosity and below which the particles infiltrate into the intra-bundle porosity.
- the particles fill, by volume, 10% - 70% of a combined volume of the intra-bundle porosity and the inter-bundle porosity.
- the particles fill, by volume, 15% - 40% of a combined volume of the intra-bundle porosity and the inter-bundle porosity.
- the remaining inter-bundle porosity is defined between the plurality of fiber bundles and the particles as deposited.
- a ceramic article includes a fiber structure that includes a plurality of fiber bundles with intra-bundle porosity and inter-bundle porosity.
- a plurality of particles has an average size with respect to the intra-bundle porosity.
- the plurality of particles is dispersed in the intra-bundle porosity and the inter-bundle porosity.
- a ceramic material is dispersed in a remaining intra-bundle porosity and a remaining inter-bundle porosity of the fiber structure.
- the plurality of particles include ceramic-based particles.
- the ceramic -based particles and the ceramic material have equivalent composition.
- the equivalent composition is silicon carbide (SiC).
- the average size of the plurality of particles is selected with respect to a size factor of the intra-bundle porosity such that the particles can fit into the intra-bundle porosity.
- the plurality of particles fill, by volume, 10% - 70% of a combined volume of the intra-bundle porosity and the inter-bundle porosity.
- the remaining inter-bundle porosity is defined between the plurality of fiber bundles and the particles.
- a method of fabricating a ceramic article according to an example of the present disclosure includes infiltrating a porosity of a porous body with a mixture of particles in a liquid carrier, removing the liquid carrier from the porous body to deposit the particles in the porous body, infiltrating a preceramic polymer into a remaining porosity between the deposited particles of the porous body, and thermally converting the preceramic polymer to a ceramic material.
- the particles fill, by volume, 10% - 70% of the porosity of the porous body.
- the particles fill, by volume, 15% - 40% of the porosity of the porous body.
- the particles and the ceramic material are silicon-based materials.
- Figure 1 illustrates a ceramic article fabricated according to this disclosure.
- Figure 2A and Figure 2B illustrate micrographs of a ceramic article fabricated according to this disclosure.
- Figures 3A and Figure 3B illustrate micrographs of a comparison ceramic article.
- the ceramic article can be a component of a gas turbine engine or other machine, but is not limited to such components.
- One example of the method includes infiltrating the porosity of a porous body with a mixture of particles in a liquid carrier, removing the liquid carrier from the porous body to deposit the particles in the porous body, removing the liquid carrier, infiltrating a preceramic polymer into the remaining porosity between the deposited particles of the porous body, and thermally converting the preceramic polymer to a ceramic material.
- the use of the particles reduces the volumetric amount of ceramic material required from conversion of the preceramic polymer, thus reducing the processing steps related to the infiltration and conversion of the ceramic material.
- the preceramic polymer can be a silicon-containing polymer.
- An example silicon-containing polymer has a silicon-containing backbone chain.
- Example silicon- containing polymers that have silicon-containing backbone chains include polysilazanes, polysilanes, polycarbosilanes, polycarbosiloxanes, polyborosilazanes and polysiloxanes, but are not limited to these.
- the silicon-containing polymer can include filler particles that can be the same or different than the particles infiltrated in the mixture with the liquid carrier, with respect to composition, but the silicon-containing polymer could alternatively be free of any filler particles.
- Example porous bodies can include fiber structures, open-pore foams or foam-like structures, or other structures that have an internal interconnected porosity.
- Fiber structures can include discontinuous or continuous fibers, and the continuous fibers may be arranged in woven, non-woven, braided, knitted or other known fiber architectures.
- the method is not limited to any particular type of porous body, although fiber structures may be desirable in many applications, such as gas turbine engines.
- FIG. 1 schematically illustrates a representative portion of a ceramic article 20, which will be used to describe further examples of the method herein.
- the method includes providing a porous body B, which here is a fiber structure that includes a plurality of fiber bundles 22.
- each fiber bundle 22 has an intra- bundle porosity 24 and an inter-bundle porosity 26.
- a fiber bundle is a group of fibers 22a that is spatially distinct from other groups of fibers.
- the fibers in a group can be twisted or untwisted, or can have other arrangements, but have interconnected spaces between individual fibers that form the intra-bundle porosity.
- the prefix "intra-” used in the context of a bundle refers to porosity inside the periphery of a group of fibers of that bundle.
- the prefix "inter-” used in the context of a plurality of bundles refers to porosity between distinct groups of fibers. Further, inter- bundle porosity and intra-bundle porosity are mutually exclusive.
- the method further includes infiltrating the intra-bundle porosity 24 and the inter-bundle porosity 26 with a mixture of particles 28 in a liquid carrier.
- the particles 28 can be selected according to the desired end-use properties of the ceramic article 20.
- the particles 28 include ceramic-based particles.
- Example ceramic -based particles can include carbide particles, nitride particles, oxide particles, boride particles, silicide particles, carbonaceous particles, oxynitride particles, oxycarbide particles and combinations thereof, but are not limited to these ceramic materials.
- the particles are silicon carbide particles.
- Metallic particles could also be used in substitution of, or in supplement to, the ceramic-based particles.
- the liquid carrier can be a solvent in which the particles can be mixed and dispersed or suspended uniformly.
- Example solvents can include water, or polar or non-polar hydrocarbon or organic solvents. The solvent will later be removed. If the solvent is to be removed by evaporation, a solvent that is readily vaporized can be used.
- a dispersant can be used to assist dispersion of the particles and maintain particle suspension during infiltration.
- Example dispersants can be small molecule or polymeric surfactants. Further example dispersants can be oxygen- or nitrogen-containing polymer surfactants that are soluble in the solvent used.
- the particles 28 have an average size, represented at 28a, that is selected with respect to at least the intra-bundle porosity 24.
- the average size 28a of the particles 28 is selected with respect to a size factor of the intra-bundle porosity 24 such that the particles 28 can fit into the intra-bundle porosity 24. If the average size of the particles 28 is too large, the particles 28 would agglomerate at the surfaces of the bundles rather than infiltrating into the intra-bundle porosity 24.
- the agglomerations would fully or substantially fully block infiltration into the intra-bundle porosity 24 and potentially debit the properties of the end article.
- the size factor of the intra-bundle porosity 24 can be, or can be factored upon, an average spacing, represented at 30, between the fibers 22a in the bundles 22.
- Such spacings can be determined by the spacing in the initial bundles 22 prior to infiltration, by experiment and microscopic inspection, or both, for example, but are not limited to such techniques.
- the liquid carrier is removed from the porous body B.
- the liquid carrier can be removed from the porous body B by evaporation. Heat can be applied to the porous body B to facilitate the removal. With or without heat, the ambient pressure around the porous body B can be reduced to facilitate the removal.
- the particles fall out of suspension and deposit in the intra-bundle porosity 24 and in the inter-bundle porosity 26.
- the liquid carrier can be fully or substantially fully removed. Further residual liquid carrier may remain in the porous body B after the removal step and may be removed secondarily in later thermal processing steps.
- the deposited particles 28 fill, by volume, 10% - 70% of a combined volume of the intra-bundle porosity 24 and the inter-bundle porosity 26. In a further example, the deposited particles 28 fill, by volume, 15% - 40% of a combined volume of the intra-bundle porosity 24 and the inter-bundle porosity 26.
- the fill percentage can be as high as practical limits dictate, which can be based on factors such as the size and type of particles 28 and the type of liquid carrier.
- An increase in the amount of the particles 28 in the liquid carrier causes an increase in the viscosity of the mixture.
- the porous body B After the removal of the liquid carrier, the porous body B includes the fiber bundles 22 and the particles 28 deposited in the intra-bundle porosity 24 and inter- bundle porosity 26.
- the selected composition of the particles is chemically unchanged relative to the initial composition of the particles 28 prior to infiltration.
- a preceramic polymer is then infiltrated, between the particles 28, into the remaining intra-bundle porosity and the remaining inter-bundle porosity.
- the remaining intra-bundle porosity is the open space, represented at 24a, between the deposited, still chemically unchanged particles 28.
- the porous body B is then thermally treated to convert the preceramic polymer to a ceramic material.
- the infiltration and thermal treatment represent one cycle or iteration of a polymer-infiltration-pyrolysis (“PIP") process. Multiple PIP process cycles can be used.
- PIP polymer-infiltration-pyrolysis
- the thermal treatment can be conducted in a controlled-temperature environment and a controlled-gas environment.
- the controlled-temperature environment can be above 1000°C, but is not limited to any particular temperature and will depend at least partially upon the type of preceramic polymer selected.
- the controlled-gas environment can also be selected at least partially based upon the type of preceramic polymer and desired end ceramic material.
- the controlled-gas environment can include a reactive or unreactive gas with respect to the preceramic polymer.
- the white background area is filled or substantially filled with the ceramic material, which embeds or substantially embeds the fiber bundles 22 and the particles 28.
- the particles 28 and the ceramic material have equivalent ceramic -based compositions.
- the fibers 22a are silicon carbide or carbon fibers
- the particles 28 are silicon carbide particles
- the ceramic material is silicon carbide.
- the particles 28 are unreactive during the thermal treatment to convert the preceramic polymer.
- the particles 28 are present in the ceramic article 20 in a chemically unchanged state with respect to the chemical composition prior to the thermal treatment to convert the preceramic polymer.
- the particles 28 can be reactive during the thermal treatment to convert the preceramic polymer, and react with one or more of the process-gas in the controlled-gas environment, the preceramic polymer, and other particles 28, to form secondary phases in the ceramic article.
- These secondary phases can be ceramic material phases, intermetallic phases, or combinations thereof.
- the particles 28 reduce the volume of the intra-bundle porosity 24 and inter-bundle porosity 26 that is occupied by the PIP-derived ceramic material.
- a thermal conversion of a preceramic polymer to a ceramic material can result in microvoids, microcracks, or the like, that occur from the shrinkage and other factors. Such features can provide points of ingress for oxygen, moisture or other substances that can contribute to debiting the properties of the article.
- the particles 28 occupy a volumetric portion of the intra-bundle porosity 24 and the inter-bundle porosity 26 and thus displace the PIP-derived ceramic.
- the PIP-derived ceramic is present in a lower volume, and in smaller volumetric domains, than it would be if the particles 28 were not used.
- the amount of such features can therefore be reduced because there is a lower volume of the PIP-derived ceramic.
- fewer microvoids and microcracks can provide an increase in the average spacing between the microvoids and microcracks and thus can reduce the degree to which such features are interconnected to form an open network for ingress of air, oxygen moisture, etc.
- the ceramic article 20 produced according to this disclosure can provide enhanced properties, such as enhanced environmental durability.
- Figure 2A and Figure 2B show micrographs of a cross-section of a ceramic article fabricated according to this disclosure. As shown in the micrographs, the article includes some cracking, but the amount of cracking is relatively low. As a comparison, Figure 3A and Figure 3B show micrographs of cross-sections of a comparison ceramic article that also has fiber bundles but was infiltrated only with a preceramic polymer and not with a mixture of particles prior to the preceramic polymer infiltration. As shown in these micrographs, there is a greater amount of cracking. Thus, the methodology disclosed herein can mitigate or reduce microcracking and thus reduce potential point of ingress for oxygen, moisture and the like.
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Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US201361897243P | 2013-10-30 | 2013-10-30 | |
PCT/US2014/061518 WO2015065764A1 (en) | 2013-10-30 | 2014-10-21 | Ceramic article and method therefor using particle infiltration and preceramic polymer infiltration |
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US20150291473A1 (en) * | 2014-04-09 | 2015-10-15 | United Technologies Corporation | Energy preparation of ceramic fiber for coating |
US20170029339A1 (en) * | 2015-07-30 | 2017-02-02 | General Electric Company | Uniformity of fiber spacing in cmc materials |
US10730203B2 (en) | 2017-09-22 | 2020-08-04 | Goodman Technologies LLC | 3D printing of silicon carbide structures |
US11274066B1 (en) | 2017-11-30 | 2022-03-15 | Goodman Technologies LLC | Ceramic armor and other structures manufactured using ceramic nano-pastes |
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US3090094A (en) * | 1961-02-21 | 1963-05-21 | Gen Motors Corp | Method of making porous ceramic articles |
FR2655977B1 (en) * | 1989-12-20 | 1993-07-09 | Onera (Off Nat Aerospatiale) | PROCESS FOR THE PREPARATION OF A CERAMIC COMPOSITE MATERIAL FIBER MATERIAL, AND COMPOSITE MATERIAL OBTAINED BY THIS PROCESS. |
US5034593A (en) * | 1990-03-23 | 1991-07-23 | W. R. Grace & Co.-Conn. | Coated welding cups |
DK0536264T3 (en) * | 1990-06-29 | 1995-05-29 | Jager Gui G De | Process for making reinforced composite materials and filament material for use in the process |
IT1284620B1 (en) * | 1996-04-05 | 1998-05-21 | Enea Ente Nuove Tec | CERAMIC MATRIX COMPOSITES, AND THEIR PRODUCTION PROCESS BY LIQUID INFILTRATION WITH POLYMER CERAMIC PRECURSORS |
US6228437B1 (en) * | 1998-12-24 | 2001-05-08 | United Technologies Corporation | Method for modifying the properties of a freeform fabricated part |
JP4484004B2 (en) | 2000-05-26 | 2010-06-16 | 株式会社Ihi | Method for producing ceramic matrix composite member |
US7378362B2 (en) * | 2000-09-29 | 2008-05-27 | Goodrich Corporation | Boron carbide based ceramic matrix composites |
JP4586310B2 (en) * | 2001-07-04 | 2010-11-24 | 株式会社Ihi | Manufacturing method of ceramic composite member |
EP1359132A1 (en) | 2002-04-30 | 2003-11-05 | European Community | Composites, applications, and process for manufacturing said composites |
US20040152581A1 (en) * | 2003-02-03 | 2004-08-05 | Bardes Bruce Paul | Ceramic article and method of manufacture therefor |
US20080265471A1 (en) | 2005-11-07 | 2008-10-30 | Colopy Curtis M | Polycrystalline Sic Electrical Devices and Methods for Fabricating the Same |
US7749568B2 (en) * | 2007-03-05 | 2010-07-06 | United Technologies Corporation | Composite article and fabrication method |
US20130122763A1 (en) * | 2009-10-06 | 2013-05-16 | Composite Tech, LLC. | Composite materials |
KR101241775B1 (en) * | 2011-07-07 | 2013-03-15 | 한국에너지기술연구원 | Method for preparing high density fiber reinforced silicon carbide composite materials |
US8900661B2 (en) * | 2011-10-03 | 2014-12-02 | United Technologies Corporation | Method of filling porosity of ceramic component |
US9701591B2 (en) * | 2011-10-12 | 2017-07-11 | United Technologies Corporation | Method for fabricating a ceramic material |
US20130167374A1 (en) | 2011-12-29 | 2013-07-04 | General Electric Company | Process of producing ceramic matrix composites and ceramic matrix composites formed thereby |
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US20180215670A1 (en) | 2018-08-02 |
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US20160264477A1 (en) | 2016-09-15 |
US9944564B2 (en) | 2018-04-17 |
WO2015065764A1 (en) | 2015-05-07 |
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